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(2-HYDROXY-PHENYL)-ACETIC ACID METHYL ESTER

  • Name(2-HYDROXY-PHENYL)-ACETIC ACID METHYL ESTER
  • CAS22446-37-3
  • Purity99%
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Product Details

Manufacturers supply cost-effective and customizable (2-HYDROXY-PHENYL)-ACETIC ACID METHYL ESTER 22446-37-3

  • Molecular Formula:C9H10O3
  • Molecular Weight:166.177
  • Vapor Pressure:0.00692mmHg at 25°C 
  • Melting Point:122-124℃ 
  • Refractive Index:1.539 
  • Boiling Point:261.9 °C at 760 mmHg 
  • PKA:9.55±0.30(Predicted) 
  • Flash Point:110 °C 
  • PSA:46.53000 
  • Density:1.181g/cm3 
  • LogP:1.10770 

(2-HYDROXY-PHENYL)-ACETIC ACID METHYL ESTER(Cas 22446-37-3) Usage

Synthesis Reference(s)

Synthetic Communications, 24, p. 2743, 1994 DOI: 10.1080/00397919408010590

InChI:InChI=1/C9H10O3/c1-12-9(11)6-7-4-2-3-5-8(7)10/h2-5,10H,6H2,1H3

22446-37-3 Relevant articles

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Levine,Eble,Fischbach

, p. 1930 (1948)

-

Regioselective Synthesis of Benzofuranones and Benzofurans

Zhang, Xiaojie,Beaudry, Christopher M.

, p. 6931 - 6936 (2021)

Reaction of 3-hydroxy-2-pyrones with nit...

Design and Synthesis of a Series of l-trans-4-Substituted Prolines as Selective Antagonists for the Ionotropic Glutamate Receptors Including Functional and X-ray Crystallographic Studies of New Subtype Selective Kainic Acid Receptor Subtype 1 (GluK1) Antagonist (2S,4R)-4-(2-Carboxyphenoxy)pyrrolidine-2-carboxylic Acid

Krogsgaard-Larsen, Niels,Delgar, Claudia G.,Koch, Karina,Brown, Patricia M. G. E.,M?ller, Charlotte,Han, Liwei,Huynh, Tri H. V.,Hansen, Stinne W.,Nielsen, Birgitte,Bowie, Derek,Pickering, Darryl S.,Kastrup, Jette Sandholm,Frydenvang, Karla,Bunch, Lennart

, p. 441 - 457 (2017)

Ionotropic glutamate receptor antagonist...

Copper-catalyzed formal [1 + 2 + 2]-annulation of alkyne-tethered diazoacetates and pyridines: Access to polycyclic indolizines

Dong, Shanliang,Hu, Wenhao,Huang, Jingjing,Qiu, Lihua,Sha, Hongkai,Xu, Xinfang

, p. 1926 - 1932 (2020)

A copper-catalyzed formal [1 + 2 + 2]-an...

Structure-Based Design and Preclinical Characterization of Selective and Orally Bioavailable Factor XIa Inhibitors: Demonstrating the Power of an Integrated S1 Protease Family Approach

Lorthiois, Edwige,Roache, James,Barnes-Seeman, David,Altmann, Eva,Hassiepen, Ulrich,Turner, Gordon,Duvadie, Rohit,Hornak, Viktor,Karki, Rajeshri G.,Schiering, Nikolaus,Weihofen, Wilhelm A.,Perruccio, Francesca,Calhoun, Amy,Fazal, Tanzina,Dedic, Darija,Durand, Corinne,Dussauge, Solene,Fettis, Kamal,Tritsch, Fabien,Dentel, Celine,Druet, Adelaide,Liu, Donglei,Kirman, Louise,Lachal, Julie,Namoto, Kenji,Bevan, Douglas,Mo, Rose,Monnet, Gabriela,Muller, Lionel,Zessis, Richard,Huang, Xueming,Lindsley, Loren,Currie, Treeve,Chiu, Yu-Hsin,Fridrich, Cary,Delgado, Peter,Wang, Shuangxi,Hollis-Symynkywicz, Micah,Berghausen, Joerg,Williams, Eric,Liu, Hong,Liang, Guiqing,Kim, Hyungchul,Hoffmann, Peter,Hein, Andreas,Ramage, Paul,D'arcy, Allan,Harlfinger, Stefanie,Renatus, Martin,Ruedisser, Simon,Feldman, David,Elliott, Jason,Sedrani, Richard,Maibaum, Juergen,Adams, Christopher M.

, p. 8088 - 8113 (2020)

The serine protease factor XI (FXI) is a...

Preparation method of carboxylic ester compound

-

Paragraph 0051-0052, (2021/03/30)

The invention relates to a preparation m...

Green Esterification of Carboxylic Acids Promoted by tert-Butyl Nitrite

Cheng, Xionglve,Jiang, Gangzhong,Li, Xingxing,Tao, Suyan,Wan, Xiaobing,Zhao, Yanwei,Zheng, Yonggao

supporting information, p. 2713 - 2718 (2021/06/25)

In this work, the green esterification o...

Insights into Ruthenium(II/IV)-Catalyzed Distal C?H Oxygenation by Weak Coordination

Bu, Qingqing,Kuniyil, Rositha,Shen, Zhigao,Gońka, El?bieta,Ackermann, Lutz

supporting information, p. 16450 - 16454 (2020/11/02)

C?H hydroxylation of aryl acetamides and...

22446-37-3 Process route

benzeneacetic acid methyl ester
101-41-7

benzeneacetic acid methyl ester

Methyl 4-hydroxyphenylacetate
14199-15-6

Methyl 4-hydroxyphenylacetate

methyl (2-hydroxyphenyl)acetate
22446-37-3

methyl (2-hydroxyphenyl)acetate

3-hydroxy-benzeneacetic acid, methyl ester
42058-59-3

3-hydroxy-benzeneacetic acid, methyl ester

Conditions
Conditions Yield
With sulfuric acid; dihydrogen peroxide; iron(III); benzene-1,2-diol; In water; at 25 ℃; Product distribution; further mediators investigated;
3-hydroxy-2-pyrone
496-64-0

3-hydroxy-2-pyrone

methyl 3-nitrobut-3-enoate
34805-49-7

methyl 3-nitrobut-3-enoate

benzofuran-2(3H)-one
553-86-6

benzofuran-2(3H)-one

methyl (2-hydroxyphenyl)acetate
22446-37-3

methyl (2-hydroxyphenyl)acetate

Conditions
Conditions Yield
With aluminum (III) chloride; 2,6-di-tert-butyl-4-methyl-phenol; In 1,2-dichloro-benzene; at 120 ℃; for 2h; Inert atmosphere;
53%
15%
With 2,6-di-tert-butyl-4-methyl-phenol; dimethylaluminum chloride; trifluoroacetic acid; In 1,2-dichloro-benzene; at 100 ℃; for 2.5h; Inert atmosphere;
30%
29%

22446-37-3 Upstream products

  • 186581-53-3
    186581-53-3

    diazomethane

  • 614-75-5
    614-75-5

    2-Hydroxyphenylacetic acid

  • 67-56-1
    67-56-1

    methanol

  • 2065-23-8
    2065-23-8

    methyl 2-phenoxyacetate

22446-37-3 Downstream products

  • 55842-25-6
    55842-25-6

    α-Phenyl-(o-carbomethoxymethyl)-phenoxy-acetat

  • 153623-45-1
    153623-45-1

    Methyl <2-(tetrahydropyranyloxy)phenyl>acetate

  • 103474-02-8
    103474-02-8

    methyl 2-(2-phenoxyphenyl)acetate

  • 76251-01-9
    76251-01-9

    methyl 2-(3,5-dibromo-2-hydroxyphenyl)acetate

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